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3,5-Heptanedione → HCID 514307, 화합물

HRID 839158
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HRID 839158 반응식
[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([CH2:10][CH2:11][CH:12]=[CH:13][CH2:14][CH2:15]I)=[CH:4][C:3]=2[O:2]1.[Li].[CH3:18][CH2:19][C:20](=[O:26])[CH2:21][C:22](=[O:25])[CH2:23][CH3:24]>CN(C)C=O>[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([CH2:10][CH2:11][CH:12]=[CH:13][CH2:14][CH2:15][CH:21]([C:20](=[O:26])[CH2:19][CH3:18])[C:22](=[O:25])[CH2:23][CH3:24])=[CH:4][C:3]=2[O:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 819233,5-HeptanedioneHCID 3028194LithiumHCID 54358058HCID 54358058, 화합물

생성물 1

HCID 514307HCID 514307, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

[I; Ar is 3,4-methylenedioxyphenyl, R0 is H, R' and R" are CH3CH2CO, Y is CH=CHCH2CH2 ] was prepared from 12.5 g. of 6-(3,4-methylenedioxyphenyl)-3-hexenyl iodide (Preparation D2) and 12.5 g. of the lithium salt of 3,5-heptanedione in 175 ml. of dimethylformamide. The product was chromatographed on silica gel and eluted with pentane-benzene (1:1) and then with chloroform-benzene (7:3). The latter brought out 7.0 g. of 4-[6-(3,4-methylenedioxyphenyl)-3-hexenyl]-3,5-heptanedione as a light amber oil.

후처리

  1. customwas prepared from 12.5 g
  2. customThe product was chromatographed on silica gel
  3. washeluted with pentane-benzene (1:1)

출처 및 근거

ORD 기록
ord-ff161409ab514a40a8a25f621c34db1c
출처 데이터셋
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04093736

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